Vaginal Mesh in Pelvic Reconstructive Surgery: Controversies, Current Use, and Complications.
In 2001, the Food and Drug Administration approved the first surgical mesh product specifically designed for the surgical repair of pelvic organ prolapse and between 2004 and 2008, the use of vaginal mesh in gynecologic surgery was at its peak. Unfortunately, the rise in transvaginal mesh use was accompanied by a surge of adverse events and mesh-related complications. As a result, the Food and Drug Administration put forth several efforts to regulate the manufacturing of vaginal mesh products. These notifications have been supported by several gynecologic societies, and recommendations now exist not only on the placement of mesh and patient selection, but also on the evaluation and management of mesh-related complications. In addition, data on outcomes following management of these complications are now emerging.
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Related Subject Headings
- Surgical Mesh
- Prosthesis Implantation
- Prosthesis Failure
- Postoperative Complications
- Pelvic Organ Prolapse
- Obstetrics & Reproductive Medicine
- Humans
- Female
- 3215 Reproductive medicine
- 1114 Paediatrics and Reproductive Medicine
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Surgical Mesh
- Prosthesis Implantation
- Prosthesis Failure
- Postoperative Complications
- Pelvic Organ Prolapse
- Obstetrics & Reproductive Medicine
- Humans
- Female
- 3215 Reproductive medicine
- 1114 Paediatrics and Reproductive Medicine